Impact of a Checklist on the Rate of Late Cancellation in Ambulatory Surgery
NCT ID: NCT01732159
Last Updated: 2015-04-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
4093 participants
INTERVENTIONAL
2012-11-30
2014-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
NONE
Study Groups
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Administration of the checklist
Patients will be contacted by phone for administration of the checklist
Checklist
he checklist will be administered to the patients by phone between 7 and 3 days before the surgery
No contact by phone
Patients who will not be contacted by phone
No interventions assigned to this group
Interventions
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Checklist
he checklist will be administered to the patients by phone between 7 and 3 days before the surgery
Eligibility Criteria
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Inclusion Criteria
* Surgery under general anesthesia or loco
* Regional or neuroleptanalgesia3. Patient contacted by phone
* Patient does not oppose his participation in the study
Exclusion Criteria
* Ambulatory surgery scheduled for orthogenic
* Ambulatory surgery scheduled for urgency
* Ambulatory surgery performed under local anesthesia
ALL
No
Sponsors
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Assistance Publique - Hôpitaux de Paris
OTHER
Responsible Party
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Principal Investigators
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Jean-Pierre BETHOUX, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Cochin Hospital
Locations
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Cochin Hospital
Paris, , France
Countries
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References
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Gaucher S, Boutron I, Marchand-Maillet F, Baron G, Douard R, Bethoux JP; AMBUPROG Group Investigators. Assessment of a Standardized Pre-Operative Telephone Checklist Designed to Avoid Late Cancellation of Ambulatory Surgery: The AMBUPROG Multicenter Randomized Controlled Trial. PLoS One. 2016 Feb 1;11(2):e0147194. doi: 10.1371/journal.pone.0147194. eCollection 2016.
Other Identifiers
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K110601
Identifier Type: -
Identifier Source: org_study_id
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